Patent classifications
C08G75/23
REACTIVE OLIGOMERS, ADDITIVE MANUFACTURING METHODS, AND ARTICLES THEREOF
A reactive oligomer has a backbone derived from at least one of polyamideimide, polyimide, polyetherimide, polyaryletherketone, polyethersulfone, polyphenylene sulfide, polyamide, polyester, polyarylate, polyesteramide, polycarbonate, polybenzoxazole or polybenzimidazole and functionalized with at least one unreacted functional group capable of thermal chain extension and crosslinking after formation of the reactive oligomer, wherein the reactive oligomer has an M.sub.n of about 250 to about 10,000 g/mol, calculated using the Carothers equation. Compositions comprising the reactive oligomer have at least one other component that includes a second reactive oligomer, an oligomer lacking unreacted functional groups capable of thermal chain extension and crosslinking, a thermoplastic polymer, a thermoplastic polymer having the same backbone repeat units as the reactive oligomer, a filler, or an additive. A method of manufacture of an article comprises heating a composition comprising the reactive oligomer at a sufficient temperature and time to shape and crosslink the reactive oligomer, including additive manufacturing.
Semicrystalline polyphenylsulfone and associated method of making and method of additive manufacturing
A semicrystalline polyphenylsulfone, has the structure Formula (I) wherein n and R are defined herein. The semicrystalline polyphenylsulfone, which exhibits a crystalline melting point in a range of 215 to 270° C., can be prepared from amorphous polyphenylsulfone using a solvent-induced crystallization method. An additive manufacturing method utilizing particles of the semicrystalline polyphenylsulfone is described. ##STR00001##
Semicrystalline polyphenylsulfone and associated method of making and method of additive manufacturing
A semicrystalline polyphenylsulfone, has the structure Formula (I) wherein n and R are defined herein. The semicrystalline polyphenylsulfone, which exhibits a crystalline melting point in a range of 215 to 270° C., can be prepared from amorphous polyphenylsulfone using a solvent-induced crystallization method. An additive manufacturing method utilizing particles of the semicrystalline polyphenylsulfone is described. ##STR00001##
Zwitterionic poly(sulfobetaine arylene ether sulfone) polymer synthesis route and applications for desalination membranes
A zwitterionic polysulfone formed from an allyl-containing monomer, a phenol-containing monomer, and an aryl-halide-containing monomer. The zwitterionic polysulfone may be incorporated into a desalination membrane.
Zwitterionic poly(sulfobetaine arylene ether sulfone) polymer synthesis route and applications for desalination membranes
A zwitterionic polysulfone formed from an allyl-containing monomer, a phenol-containing monomer, and an aryl-halide-containing monomer. The zwitterionic polysulfone may be incorporated into a desalination membrane.
Methods for making poly(aryl ether sulfone) polymers and polymer compositions and articles including the same
Described herein are methods for making poly(aryl ether sulfone) (“PAES”) polymers and polymer compositions including the PAES polymers. The method includes reacting a first monomer and a second monomer in a reaction mixture including a base. In some embodiments, the first monomer, second monomer and base can be selected such that halogen salts are not formed during the reacting. In some embodiments, the method can also be a solvent free process. The PAES polymer and polymer compositions can be desirable in many application settings including, but not limited to, electronic components.
Methods for making poly(aryl ether sulfone) polymers and polymer compositions and articles including the same
Described herein are methods for making poly(aryl ether sulfone) (“PAES”) polymers and polymer compositions including the PAES polymers. The method includes reacting a first monomer and a second monomer in a reaction mixture including a base. In some embodiments, the first monomer, second monomer and base can be selected such that halogen salts are not formed during the reacting. In some embodiments, the method can also be a solvent free process. The PAES polymer and polymer compositions can be desirable in many application settings including, but not limited to, electronic components.
Process for preparing functionalized poly(aryl ether sulfones) polymers and block copolymers resulting therefrom
Poly(aryl ether sulfones) (PAES) polymers (P1) which are functionalized with reactive functional groups on at least one end of the PAES polymer, a process for preparing the PAES polymers (P1), a process for preparing block copolymers (P2) using the functionalized poly(aryl ether sulfones) (PAES) polymers (P1) and the block copolymers (P2) obtainable by such process
Process for preparing functionalized poly(aryl ether sulfones) polymers and block copolymers resulting therefrom
Poly(aryl ether sulfones) (PAES) polymers (P1) which are functionalized with reactive functional groups on at least one end of the PAES polymer, a process for preparing the PAES polymers (P1), a process for preparing block copolymers (P2) using the functionalized poly(aryl ether sulfones) (PAES) polymers (P1) and the block copolymers (P2) obtainable by such process
Thermoplastic resin composition and molded article formed therefrom
A thermoplastic resin composition of the present invention comprises: about 5 wt % to about 35 wt % of a modified polyaryletherketone resin comprising a repeat unit represented by chemical formula 1; about 5 wt % to about 35 wt % of a polyether ether ketone resin; about 20 wt % to about 40 wt % of a polyphenylsulfone resin; and about 15 wt % to about 50 wt % of glass fibers. The thermoplastic resin composition has good properties in terms of adhesion to metals, impact resistance, and so on.